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SSCOR/board 23001

by Sscor, Inc.

SSCOR/board 23001 is an emergency airway clearance suction system (FDA Class II; FDA product code GCX, Apparatus, Suction, Operating-Room, Wall Vacuum Powered) made by Sscor, Inc., listed in FDA GUDID since 13 Feb 2017 (UDI-DI B245230010), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB245230010 UDI-DI Date13 Feb 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
SSCOR/board
Generic name
Emergency airway clearance suction system, electric
Model / reference
23001
Primary DI / UDI-DI
B245230010
FDA product code
GCX
GMDN term
Emergency airway clearance suction system, electric
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Emergency airway clearance suction system, electric

Similar devices

Other devices filed under FDA product code GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered).

Other devices from Sscor, Inc.

See all devices from Sscor, Inc. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)